Genomic variant #0000000070

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.7577918A>G
Reference -
DB-ID CAMTA1_000062
dbSNP ID rs10492961
Frequency 0.3559
Homozygous 48
Heterozygote 146
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAMTA1 NM_015215.3 ./. - c.511-62482A>G - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin